| Summary: | Catechols are antioxidants and radical scavengers with a broad medical potential. 4-Methylcatechol (<b>1b</b>) and 4-ethylcatechol (<b>2b</b>) (occurring in some traditional fermented and smoked foods) activate the cell defense against oxidative stress. We examined the biocatalyzed reactions towards 4-<i>n</i>-alkylcatechols with different side chains length, which is a factor important for the biological activities of catechols. 4-<i>n</i>-Alkylcatechols with methyl through heptyl side chains (<b>1b</b>–<b>7b</b>) were obtained in one pot by (i) oxidation of phenols <b>1a</b>–<b>7a</b> with tyrosinase from <i>Agaricus bisporus</i> followed by (ii) reduction of <i>ortho</i>-quinones (intermediates) with L-ascorbic acid sodium salt. The conversions decreased with increasing side chain length. The preparative reactions were carried out with substrates <b>1a</b>–<b>5a</b>. The isolated yields of the purified products decreased from 59% in <b>2b</b> to 10% in <b>5b</b> in correlation with logP of the substrates. Homology modeling indicated that the affinities of two tyrosinase isoforms (PPO3 and PPO4) to the substrates with side chains longer than C2 decreased with increasing side chain length. This was probably due to steric limitations and to missing interactions of the side chains in the active sites. We envisage using the model to predict further substrates of tyrosinase and testing the products, catechols, for radical-scavenging and biological activities.
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